It all came too late for me

A significant factor,aside from the bullying,in my developing a SMI was the intense anxiety of not wanting to disappoint my parents and yet being acutely aware that I lacked the non academic/independent living skills to cope with going to university. Nowadays though the system could be better, it's  better equipped to help and support a 2020s version of me.A combination of there being no such support in the mid 1970s, and it taking till I was 60 for it to be acknowledged I had  such difficulties,  meant that,combined with fear of bullying,further education was not a realistic option.

Sometimes I feel worthless because of it. I wonder how many of my generation were in the same boat and, like me, never had the necessary help and support.

Parents
  • I was diagnosed with ASC at 59. I had what I now recognise was a panic attack in my first A-level exam. It lasted about 10 minutes or so, then I started writing at top speed. I did go to university, there is a streak of stoicism in my family that stood me in good stead, if you say you are going to do something, then you just do it. I had problems, in the first couple of weeks I could hardly eat in the hall refectory due to nervousness, and anxiety in the build up to exams was a recurring problem. However, I coped, I functioned sub-optimally, but I functioned. For the first and only time in my life I had a group of friends numbering around half a dozen - all through my school days I tended to have only a couple of friends at any one time. I got a degree, not quite as good as I deserved, I was an undiagnosed autistic after all, and had recurring headache problems, due to sinus issues, that affected my ability to study. Ironically, I now recognise that my autism inhibited my ability to report my physical health problems to the university and thereby receive some leniency in assessment and marking.

    I eventually got a job in a university in scientific research and went on to get further degrees - incidentally, research degrees, masters and doctorates, are much easier for autistics than undergraduate degrees. All the time I coped, largely because I expected myself to cope and did not see not coping as an option. It did come at a cost, I could not understand why things seemed to be so much easier for other people than they were for me, why I was limited in some ways, and why I was often exhausted. The first time I ever had any interaction with a medical professional for anything other than a physical problem was in my autism assessment.

Reply
  • I was diagnosed with ASC at 59. I had what I now recognise was a panic attack in my first A-level exam. It lasted about 10 minutes or so, then I started writing at top speed. I did go to university, there is a streak of stoicism in my family that stood me in good stead, if you say you are going to do something, then you just do it. I had problems, in the first couple of weeks I could hardly eat in the hall refectory due to nervousness, and anxiety in the build up to exams was a recurring problem. However, I coped, I functioned sub-optimally, but I functioned. For the first and only time in my life I had a group of friends numbering around half a dozen - all through my school days I tended to have only a couple of friends at any one time. I got a degree, not quite as good as I deserved, I was an undiagnosed autistic after all, and had recurring headache problems, due to sinus issues, that affected my ability to study. Ironically, I now recognise that my autism inhibited my ability to report my physical health problems to the university and thereby receive some leniency in assessment and marking.

    I eventually got a job in a university in scientific research and went on to get further degrees - incidentally, research degrees, masters and doctorates, are much easier for autistics than undergraduate degrees. All the time I coped, largely because I expected myself to cope and did not see not coping as an option. It did come at a cost, I could not understand why things seemed to be so much easier for other people than they were for me, why I was limited in some ways, and why I was often exhausted. The first time I ever had any interaction with a medical professional for anything other than a physical problem was in my autism assessment.

Children
  • You write : 

    ’ It did come at a cost, I could not understand why things seemed to be so much easier for other people than they were for me, why I was limited in some ways, and why I was often exhausted.’

    That’s it in a nutshell really. Undiagnosed, feeling like everything is a struggle, feeling confused and so very tired most of the time. That’s been my life basically.